Study of Rivaroxaban for CeREbral Venous Thrombosis

PHASE2CompletedINTERVENTIONAL
Enrollment

55

Participants

Timeline

Start Date

March 12, 2019

Primary Completion Date

October 5, 2022

Study Completion Date

October 5, 2022

Conditions
Cerebral Venous Thrombosis
Interventions
DRUG

Rivaroxaban

Rivaroxaban 20 mg daily (15 mg daily in participants with a CrCl 30-49 mL/min as per the Cockroft-Gault equation)

DRUG

Standard of care

Accepted standard of care as per American Heart Association/American Stroke Association Guidelines (initial use of unfractionated heparin or low-molecular weight heparin with transition to an oral vitamin K antagonist or continuation with low-molecular weight heparin) with choice of agent at the treating physician's discretion.

Trial Locations (11)

T2N 2T9

Foothills Medical Centre, Calgary

T6G 2B7

University of Alberta Hospital, Edmonton

V1Y 1T2

Kelowna General Hospital, Kelowna

V5Z1M9

Vancouver General Hospital, Vancouver

L8L 2X2

Hamilton Health Sciences Centre, Hamilton

N6A 5W9

London Health Sciences Centre, London

K1Y 4E9

The Ottawa Hospital Research Institute, Ottawa

M4N 3M5

Sunnybrook Health Sciences Centre, Toronto

M5T 2S8

Toronto Western Hospital, Toronto

H2X 0A9

Centre hospitalier de l'Université de Montréal, Montreal

S7N 0W8

Royal University Hospital, Saskatoon

All Listed Sponsors
lead

University of British Columbia

OTHER

NCT03178864 - Study of Rivaroxaban for CeREbral Venous Thrombosis | Biotech Hunter | Biotech Hunter